Critical role of FOXO3a in carcinogenesis

Abstract

FOXO3a is a member of the FOXO subfamily of forkhead transcription factors that mediate a variety of cellular processes including apoptosis, proliferation, cell cycle progression, DNA damage and tumorigenesis. It also responds to several cellular stresses such as UV irradiation and oxidative stress. The function of FOXO3a is regulated by a complex network of processes, including post-transcriptional suppression by microRNAs (miRNAs), post-translational modifications (PTMs) and protein–protein interactions. FOXO3a is widely implicated in a variety of diseases, particularly in malignancy of breast, liver, colon, prostate, bladder, and nasopharyngeal cancers. Emerging evidences indicate that FOXO3a acts as a tumor suppressor in cancer. FOXO3a is frequently inactivated in cancer cell lines by mutation of the FOXO3a gene or cytoplasmic sequestration of FOXO3a protein. And its inactivation is associated with the initiation and progression of cancer. In experimental studies, overexpression of FOXO3a inhibits the proliferation, tumorigenic potential, and invasiveness of cancer cells, while silencing of FOXO3a results in marked attenuation in protection against tumorigenesis. The role of FOXO3a in both normal physiology as well as in cancer development have presented a great challenge to formulating an effective therapeutic strategy for cancer. In this review, we summarize the recent findings and overview of the current understanding of the influence of FOXO3a in cancer development and progression.

Background

Forkhead box (FOX) proteins are evolutionarily conserved transcription factor family of proteins, which are characterized by their forkhead winged helix-turn-helix DNA binding domain composed of three α–helices and two loop or “wing” domains. Currently, more than 2000 members have been found in this family of transcription factors based on sequence homology, which are ubiquitously expressed across a range of species from yeast to human [1, 2]. FOX proteins regulate a wide spectrum of biological processes involved in normal homeostasis and development [3, 4]. Although the forkhead DNA binding domain with ~ 100 amino acid residues is highly conserved, the other domains are very divergent in FOX proteins. So they have very different binding specificities and cellular effects. According to additional domains and sequence conservation, FOX family is further grouped into various subfamilies, namely FOXM, FOXK, FOXA and FOXO families [5–7].

The forkhead box class O (FOXO) family is a ubiquitously expressed transcription factor that plays important role in higher organisms. The first member of this family with fork head was described in Drosophila, which plays key roles in the terminal development of Drosophila embryo [8]. The mammalian system consists of four members, namely FOXO1, FOXO3a, FOXO4, and FOXO6, which are known to be regulated by the phosphoinositol-3-kinase (PI3K)-PKB signaling pathway [9–11]. FOXO family has been shown to regulate developmental processes and energy metabolism as well as tumorigenesis in many tissues. All these functions are mediated by the specific activation of a coordinated transcriptional program [12]. The deregulation of FOXO functions will cause uncontrolled cell proliferation and accumulation of DNA damage, which results in carcinogenesis.

The member of FOXO subfamily, FOXO3a, also known as FOXO3 or forehead in rhabdomyosarcoma-like 1 (FKHRL1), was first identified in human placental cosmid. The FOXO3a gene is located on chromosome 6q21 [13] and it plays vital role in regulating a variety of cellular processes through targeting the expression and activity of effector genes. The subcellular localization of FOXO3a is important for its activities and functions [14]. The phosphorylation of FOXO3a leads to its translocation from nucleus to cytoplasm, where it associates with 14–3-3 protein and this binding prevents its reentry into the nucleus [15, 16]. In this review, we focus on the recent findings and important progress made in identification of FOXO3a functions and its target molecules and we have also presented an overview of the current understanding of the influence of FOXO3a activity on cancer.

Overview: Structure, regulation and function of FOXO3a

Structural domains of FOXO3a

FOXO3a is approximately 71 kDa in size and its structure is conserved across different species. FOXO3a contains five domains: a highly conserved forkhead winged helix-turn-helix DNA binding domain (FKH), two nuclear localization sequence (NLS), a nuclear export sequence (NES) and C-terminal transactivation domain (TAD) (Fig. 1). Among the FOXO family members, many of these regions are highly conserved. A highly conserved Forkhead Domain is primarily responsible for direct interaction between FOXO3a and DNA, which also mediates its interaction with Estrogen receptor α (ERα) [17] and p53 [18]. NLS domain is required for the translocation of FOXO3a from cytoplasm to nucleus and it also mediates the release of FOXO3a from nucleus [19]. TAD domain in C-terminal is vital for the transactivation of FOXO3a target genes.

Fig. 1.

Structure of human FOXO3a. Letters within the bar indicate structural domains. The well-known proteins interacting with FOXO3a are shown above the lines at the corresponding domains. Only representatives of FOXO3a-interacting proteins are shown. FKH, forkhead winged helix-turn-helix DNA binding domain; TAD, transactivation domain; NLS, nuclear localization sequence; NES, nuclear export sequence

Regulation of FOXO3a activity

MiRNA pathways contribute to post-transcriptional regulation of FOXO3a

MicroRNA (miRNA) is a kind of short single-stranded non-protein-coding RNA molecules that negatively regulates the gene expression at the posttranscriptional level by repressing translation and/or promoting mRNA degradation [20, 21]. There are more than 30% of genes are regulated by miRNA in human system [22]. The 3′-untranslated region (3′-UTR) of FOXO3a mRNA harbors several miRNA target sequences. Many miRNAs modulate the expression of FOXO3a proteins under various pathological conditions. FOXO3a is directly targeted by miR-155 in ischemic renal diseases and some types of cancer. Experimental studies revealed that the overexpression of miR-155 down-regulates the expression of FOXO3a protein, while knockdown of miR-155 increases FOXO3a expression [23–27]. FOXO3a is also regulated by other miRNAs, including miR-132, miR-212 and miR-223. They directly bind to FOXO3a 3′-UTR and inhibit the expression of FOXO3a. The de-repression of FOXO3a by microRNA-132 and 212 cause neuronal apoptosis in Alzheimer’s disease [28]. In addition, miR-132 and 223 promote pathogenesis of inflammatory bowel disease by negatively regulating FOXO3a [29]. In glioblastoma cells, the overexpression of miR-27a can inhibit the expression of FOXO3a protein and its transcriptional activity, while the inhibition of miR-27a increases the expression and activity of FOXO3a, which indicates that FOXO3a is a target of miR-27a [30]. In traumatic brain injury condition, miR-27a displays neuroprotective effect by directly targeting FOXO3a-mediated neuronal autophagy [31]. In human breast cancer and Idiopathic pulmonary fibrosis, miR-96 directly targets the 3′UTR of the FOXO3a mRNA, which consequently decreases the expression of FOXO3a targets (p27 and p21) and increasing cyclin D1 [32, 33]. FOXO3a can also be directly regulated by other miRNAs, such as miR-30d, miR-182, miR-592, miR-1307 and 29a [34–38]. Modulation of FOXO3a by anti-miR strategies may prove useful to promote apoptosis. In addition to the direct regulation of miRNA, FOXO3a activity also can be regulated by miRNAs in an indirect manner. For instance, miR205 upregulates AKT dependent activation of FOXO3a in lung cancer cell via suppressing PTEN [39]. Therefore, to explore the comprehensive of network of microRNAs and FOXO3a, further research is required to design FOXO3a based strategies for better chemotherapeutics.

Importance of post-translational modifications in regulation of FOXO3a

Post-translational modifications (PTMs) is the fundamental process for the regulation of proteins’ functions that cause changes in their subcellular location, molecular half-life, DNA-binding affinity and/or interaction with other cellular proteins. The common PTMs include phosphorylation, acetylation, methylation, ubiquitination, sumoylation, neddylation, glycosylation, sulphation and prenylation. The activity of FOXO3a can be regulated by multiple types of PTMs including phosphorylation, acetylation, ubiquitination and methylation [9, 40, 41]. These reversible PTMs alter the translocation of FOXO3a, influence its DNA binding affinity, and change the pattern of transcriptional activity at specific target genes sites [42, 43]. These modifications in FOXO3a occur consecutively by various combinations of enzymes and signaling molecules.

The primary mechanism of regulation of FOXO3a activity and its target genes is by controlling the translocation of FOXO3a between nucleus and cytoplasm, which can be achieved by phosphorylation by a series of kinases. The protein kinases such as protein kinase B (PKB), extracellular signal-regulated kinase (ERK), Serum-and glucocorticoid-inducible kinases (SGK) and IκB kinase isoform β (IKKβ) promote the nuclear export of FOXO3a [44–47]. Whereas, poly(ADP-ribosyl)ated by PARP1 dependent phosphorylation facilitates its exclusion from the nucleus [48]. After the cytoplasmic retention, FOXO3a is ubiquitinated and then degradated by proteasome [45]. The sites for PTMs in FOXO3a is well defined and activation of these kinases normally correlates with loss of nuclear FOXO3a. However, the phosphorylation of FOXO3a by p38, Macrophage stimulating 1 (MST1) and AMPK promote its nuclear entry and increase its transcriptional activity [49–51]. Given the fact that the balancing of nuclear import and export is very important to maintain FOXO3a functions, the loss of this balance leads to development and progression of various diseases including cancer.

The PTMs of nuclear FOXO3a regulates its transcriptional activity by changing DNA binding affinity and promoter binding specificity. In nucleus, FOXO3a is acetylated by p300 and CREB-binding protein (CBP) and it is deacetylated by SIRT1 and SIRT2. Interestingly, SIRT1 mediated deacetylation changes the DNA binding affinity of FOXO3a [52], while deacetylation by SIRT2 increases its DNA-binding activity [53]. The coactivator-associated arginine methyltransferase 1 (CARM1) dependent methylation of FOXO3a is required for its activation in the nucleus [40]. A molecular study found that the methylation of FOXO3a at K270 leads to the loss of DNA binding ability and it reduces FOXO3a-mediated apoptosis. Many PTMs of FOXO3a can interact with each other, and function in combination or compete with each other. Therefore, exploring the FOXO code is essential to understand the function and mechanism of FOXO3a.

Alternative protein–protein interactions modulate FOXO3a activity

The activity of FOXO3a can be modulated by other proteins via protein-protein interactions. As a transcription factor, FOXO3a interacts with co-regulators (co-activators or co-repressors) and general transcription factors to regulate the gene expression of its target. In neuronal cells, C/EBP homologous protein (CHOP) directly interacts with FOXO3a in response to endoplasmic reticulum stress and that increases the transcription activity of FOXO3a and inducing the expression of FOXO3a target genes Puma and Bim [54]. In many cancer cell lines, c-Myc binds with FOXO3a and this interaction represses FOXO3a-mediated activation of the p27 promoter as evident from consistent with the inverse patterns of their expression in a diverse group of human cancers [55]. In MCF-7 cells, latency associated nuclear antigen 2 (LANA2) functionally interacts with FOXO3a and inhibits the transactivation of Bim promoter mediated by FOXO3a [56]. In normal lympho-blasts and HeLa cells treated with H₂O₂, forms a complex with FOXO3a by direct binding with FANCD2 in response to oxidative stress [57]. In COS-7 cells, the interaction of p53 with FOXO3a suppresses transcriptional activity of FOXO3a. In fact, p53 decreases the expression of apoptosis-inducible genes such as Bim and Bcl6, but it does not affect the expression of p27 and Cyclin G2 [58]. In HeLa cells, FOXO3a is de-phosphorylated by PP2A interaction, which results in the rapid nuclear translocation and transcriptional activation of FOXO3a [59]. In Gastric Cancer Cells, the complex of RUNX3 and FOXO3a participates in the induction of apoptosis by activating FOXO3a target gene Bim [60]. In the Mitochondria, the interaction of SIRT3 with FOXO3a increases FOXO3a DNA-binding activity as well as FOXO3a dependent gene expression [61].

Functions of FOXO3a

FOXO3a is a central transcription factor that mediates multiple physiological and pathological processes by inducing transcription of target genes involved in apoptosis [62], proliferation [63], cell cycle progression [64], survival [65] and DNA damage [66] (Fig. 2). It also respond to several cellular stresses such as UV irradiation [67] and oxidative stress [68, 69]. Besides, FOXO3a is strongly associated with human longevity [70]. FOXO3a is also involved in the regulation of autophagy process in muscle and in cancer cells [71, 72]. The multiple functions of FOXO3a indicate that deregulation of FOXO3a expression and/or activity can lead to various diseases, particularly cancer. Indeed, the overexpression of FOXO3a has been shown to inhibit tumorigenesis in breast cancer [17, 73]. The export of FOXO3a from nucleus seems to be related to poor survival of breast cancer patients [73]. In this context, the tumor suppressor function of FOXO3a is also well defined in other type of cancers.

Fig. 2.

The functions and regulation of FOXO3a. The non-phosphorylated form of FOXO3a located in nucleus actively mediates multiple cellular processes, including cell apoptosis, proliferation, cell cycle, survival and DNA damage by inducing transcription of its target genes depends on the upstream stimuli. The growth factor signaling induced activation of protein kinases such as PKB, ERK, SGK, IKKΒ terminate FOXO3a activity by phosphorylation (in active form). The phosphorylated FOXO3a binds with 14–3-3 protein, which consequently leads to nuclear export of FOXO3a. In the cytoplasm, FOXO3a is ubiquitinated and degraded in a proteasome-dependent manner

FOXO3a in diseases development

FOXO3a and its role in non-neoplastic diseases

The dysregulation of FOXO3a has been implicated in many pathological processes. FOXO3a play a crucial role in neurological disorders such as Alzheimer’s diseases, Lewy body dementia, Parkinson’s diseases, motor neuron disease and acute spinal cord injury. FOXO3a also associated with the development of heart disease, muscle atrophy, and premature ovarian failure.

Alzheimer’s disease (AD) is a most common form of age-associated dementia, which is a multifactorial and progressive neurodegenerative disorder. The mRNA and protein levels of FOXO3a are significantly up-regulated, and most of the its target genes are increased in AD brains, which indicates that the FOXO3a signaling pathway contributes to AD neurodegeneration [28]. In the Tg2576 mouse model of AD, the inactivation of FOXO3a had attenuated AD-type amyloid neuropathology. In primary neuron cultures derived from Tg2576 mouse embryos, a constitutively active form of FOXO3a promotes AD amyloid-β peptide (Aβ) levels by inhibiting non-amyloidogenic α-secretase activity, which indicates the existence of an inverse correlation between FOXO3a activity and Q Aβ amyloidosis [74].

Parkinson’s disease (PD) and Lewy body dementia (LBD) are recognized as disorders of protein aggregation and inclusion body formation. The increased activity and expression of FOXO3a is intimately associated with Lewy bodies and Lewy neurites in the brain tissue of LBD and PD. In fact, the localization of FOXO3a to Lewy bodies result in the degeneration of neurons [75].

The cardiovascular problems and its associated complications are the leading cause of mortality worldwide. FOXO3a acts as a negative regulator of cardiomyocyte size in the cardiac tissue [76]. Our previous study demonstrated that FOXO3a inhibits cardiomyocyte hypertrophy by transcriptionally targeting catalase [77]. In pathological hypertrophy and heart failure, FOXO3a drives the expression of BNIP3 and induces mitochondrial apoptosis and mitophagy [78]. FOXO3a can inhibit cardiomyocyte hypertrophy by suppressing the expression of p21, Cat and Atrogin-1 [77, 79, 80], which are involved in hypertrophic response.

Recent studies demonstrate that FOXO3a up-regulates the expression of the atrophy-related ubiquitin ligases atrogin-1 and muscle Ring Finger-1, which induce a rapid loss of muscle mass [81, 82]. Hsp70 and SAPKs inhibit the activity of FOXO3a and prevent skeletal muscle atrophy [83, 84]. On the other hand, FOXO3a promotes cell survival pathway in aortic vascular smooth muscle cells. However, its deregulation due to a reduction of IGF-1R signaling may promote apoptosis during atherosclerosis [85]. FOXO3a is a critical regulator of follicular activation. A study in mice with ovarian phenotype of FOXO3a^−/−showed a similar phenotype with the human premature ovarian failure (POF). A mutation screening in POF patients have revealed that there are eight variants in FOXO3a and three of them are resulting in amino acid substitutions, which indicates that FOXO3a is a candidate gene for POF in human [86]. After acute spinal cord contusion injury, a significant decrease in the expression of FOXO3a favors axonal regeneration and glial cell proliferation by reduction in the expression of its target protein p27^kip1, which indicates that FOXO3a has a detrimental role in nervous system lesion and repair [87]. In contrast, the pharmacological or genetic activation of FOXO3a protects neurons from damage caused by motor neuron diseases [88].

Implication of FOXO3a in carcinogenesis

It is well known that FOXO3a has a crucial role in apoptosis, cell proliferation, DNA damage and resistance to oxidative stress, and thus its deregulation of FOXO3a is highly associated with a series of malignancies [60, 89–103] (Table 1). In most of the malignant cells, the deregulation of FOXO3a is mainly through aberrant PTMs.

Table 1.

Functional roles of FOXO3a pathway in different types of cancer

Cancer types	Key message(s)	Ref.
Breast cancer	Dephosphorylation of FOXO3a induced by Aplysin suppresses tumor growth by inhibiting cell proliferation and promoting apoptosis in cancer cells.	[89]
Prostate cancer	Deregulation of FOXO3a promotes prostate cancer progression in TRAMP mice.	[90]
Acute myeloid leukemia	Dephosphorylation of FOXO3a induced by hypomethylating agents promote apoptosis by upregulation of BIM and PUMA expression.	[91]
Colon cancer	Activation of FOXO3a by aldose reductase induces human colon cancer cell apoptosis by upregulating both DR5 and DR4.	[92]
Lung cancer	Deregulation of FOXO3a promotes DNMT3B overexpression leading to tumor growth in lung cancer.	[93]
Glioma	A high expression of FOXO3a is associated with glioblastoma progression and FOXO3a level independently indicates poor prognosis in Glioma patients.	[94]
Thyroid cancer	Nuclear FOXO3a promotes cell cycle progression by transcriptional upregulation of cyclin A1 and accelerates proliferation of human ATC cells.	[95]
Lung adenocarcinoma	FOXO3a gene inactivation occurs frequently in carcinogen-induced lung adenocarcinoma.	[96]
Oral squamous cell carcinoma	Constitutively active form of FOXO3a induces significant G1-phase arrest and apoptosis in OSCC cells	[97]
Neck cancer	Tumor patients with low FOXO3a expression have a poor prognosis compared with patients with high FOXO3a.	[98]
Urothelial cancer	FOXO3a suppresses invasiveness of urothelial cancer through regulation of Twist1, YB-1 and E-cadherin.	[99]
Osteosarcoma	Activation of FOXO3a by ionizing radiation induces cell apoptosis in osteosarcoma.	[100]
Bladder cancer	Upregulation of FOXO3a by Nkx2.8 suppresses bladder cancer proliferation.
Gastric cancer	FOXO3a cooperates with RUNX3 to induce apoptosis by activating Bim in gastric cancer cells.	[60, 101]
Neuroblastoma	Inactivation of FOXO3a by AKT is essential for neuroblastoma cell survival.	[102]
Ovarian cancer	Inhibition of FOXO3a phosphorylation by BrMC upregulates Bim expression and leads to apoptosis in ovarian cancer cells.	[103]

Deregulation of FOXO3a phosphorylation

FOXO3a is phosphorylated by several upstream kinases, such as Akt, ERK, SGK, IKKβ and IKBKE [104]. The phosphorylated FOXO3a is expelled from nucleus by binding with 14–3-3 proteins and through exportins. In the cytoplasm, FOXO3a is further ubiquitinated and then degradated by an ubiquitin/proteasome-dependent manner [105]. The deregulation of these kinases are frequently observed in different kinds of cancers and that contributes to the progression of carcinogenesis by promoting the nuclear-to-cytoplasm translocation and/or ubiquitin/proteasome dependent degradation of FOXO [106].

The role of JNK in cancer is still in debate that has pro-oncogenic as well as tumor-suppressor roles in cancer tissue depends on the upstream signaling. Its expression and/or activity is dysregulated during carcinogenesis [107]. The abnormal activation of JNK by UV irradiation inactivates ERK and PKB, which, in turn, leads to cell death by increased activity of nuclear FOXO3a and Bim expression [67]. IKK plays important roles in chromatin remodeling, cell cycle progression and nuclear factor κB (NFκB) signaling pathway, which is involved in the development of disorders, including cancer [108]. IKK directly interacts with and phosphorylates FOXO3a independent of PKB, and that causes the degradation of FOXO3a. The cytoplasmic level of FOXO3a correlates with the expression of IKKβ in many types of tumor. The negative regulation of FOXO3a by IKK plays a key role in promoting malignant cell growth and tumorigenesis [73]. The RAS–ERK signaling pathway can be activated by a wide range of extracellular growth signals that is known to play a crucial role in differentiation, proliferation and tumor progression. A constitutively active ERK phosphorylates FOXO3a and consequently promotes its degradation, thereby ERK pathway contributing to carcinogenesis [45].

The PI3K–PKB signaling pathway is involved in many fundamental cellular functions such as proliferation, growth, and survival. The PI3K–PKB signaling pathway is frequently dysregulated by different types of cellular stress stimuli or toxic insults. For example, the activation of PI3K-PKB by upstream activators or amplification of PI3K/PKB genes lead to uncontrolled activation of PKB pathway and it contributes to carcinogenesis [109]. PKB abnormally activated by some protein kinases in leukemia cells. The Fms-like tyrosine kinase-3 (FLT3) receptors within-frame internal tandem duplications (ITD) acts as a upstream for PKB signaling that have been found in about 30% of the patients with acute myeloid leukemia. FLT3-ITD receptors exhibit constitutive tyrosine kinase activity without its ligand binding. Thus, the expression of FLT3-ITD results in relentless activation of PKB and concomitant phosphorylation of FOXO3a in leukemia cells. The phosphorylation of FOXO3a induces its translocation from nucleus to cytoplasm, which in turn leads to suppression of the expression of its target genes p27^Kip1 and Bim [110]. Similarly, the nucleophosmin–anaplastic lymphoma kinase (NPM-ALK) is a fusion protein kinase which is generated in 30–50% of patients with advanced-stage anaplastic large-cell lymphoma. InBa/F3 cells, the inducible or constitutive expression of NPM-ALK results in concomitant activation of AKT and phosphorylation of FOXO3a, a frequently observed cellular event in anaplastic large-cell lymphoma [111]. A study in mouse model has revealed that Pml deficiency fails to recruit PP2a, PKB phosphatase into PML nuclear bodies, which leads to the accumulation of nuclear phosphor-Akt and nuclear exclusion of FOXO3a. This results in progression of tumorigenesis process in the prostate [112].

The phosphatase and tensin homologue deleted on chromosome 10 (PTEN) is a dual function lipid and protein phosphatase, which was originally identified as a tumor-suppressor. PTEN negatively regulates the PI3K-PKB pathway by dephosphorylation of PI(3,4,5)P3 and down-regulation of PI3K activity. The inactivation of PTEN due to mutations is observed in many primary tumors, such as thyroid, prostate, uterus and breast [109]. The mutation or loss of PTEN activity results in aberrant activation of PKB signaling and nuclear export of FOXO3a during carcinogenesis. In experimental studies found that FOXO3a in PTEN-negative tumors result in cell cycle arrest and apoptosis [3]. Thus, the inactivation of FOXO3a by deregulation of its upstream phosphokinases is crucial for the nuclear export of FOXO3a and acceleration of carcinogenesis. Taken together, these studies strongly suggest that the imbalance between kinases and phosphatases can significantly affect the cellular processes through inhibiting FOXO3a activity, and the alteration of these kinases and phosphatases may cause the dysregulation of FOXO3a leading to carcinogenesis.

Effectors of FOXO3a deregulation

Multiple mechanisms have been associated with FOXO3a dysregulation and carcinogenesis due to the fact that it governs many genes involved in apoptosis (such as Bim, Noxa, Puma, FasL and TRAIL) and cell proliferation (including p21, p27, p130, Cyclin G2 and GADD45) [113]. Our previous study demonstrated that FOXO3a binds to the promoter region of miR-21 and suppresses its promoter activity in human neuroblastoma cells. Fas ligand, a pro-apoptotic factor, is a downstream target of miR-21. Foxo3a inhibits miR-21 transcriptionally which results in to the up-regulation of Fas ligand, and hence initiate the apoptosis [114]. The transcriptional repressor MXI1-SRα is a direct target of FOXO3a, which mediates the repression of MYC activity by FOXO3a [115]. These results indicate that FOXO3a dysregulation contributes to carcinogenesis through directly regulating its target genes expression, and/or affecting its downstream effectors, such as MXI1-SRα.

FOXO3a coordinately works with other transcription factors in cancer

FOXO3a has the ability to suppress cancer cell proliferation by down-regulating the expression of several ER-relates genes, which are involved in cell cycle progression. The direct interaction of FOXO3a with ER-α and ER-β proteins causes inhibition of 17β-estradiol (E2)-dependent ER gene transcriptional activities. In ER-positive breast cancer MCF-7 cells, the overexpression of FOXO3a up-regulates the expression of the cyclin-dependent kinase inhibitors (including p21^Cip1, p27^Kip1, and p57^Kip2), which results in the repression of the growth and survival of MCF-7 cells [17]. Molecular studies show that there are several structural and functional similarities between p53 and FOXO3a. Both p53 and FOXO3a control cell cycle progression and DNA damage repair, and both of them can be post-translationally modified by acetylation and phosphorylation. They have regulate a range of genes in common. Thus, there is functional cross talk between these two transcription factors. p53 promotes the expression of SGK, while SGK phosphorylates and inhibits FOXO3a. On the other hand, FOXO3a relieves p53-mediated repression of SIRT1 expression, which, in turn, deacetylates p53 [116]. The transcription factor, RUNX3, is a candidate tumor suppressor that mediates apoptosis and cell growth inhibition in gastric epithelial cells that interacts with FOXO3a and this complex activates Bim to induce apoptosis [60]. FOXO3a also cooperate with other members of forkhead-box transcription factors. For example, FOXO3a interacts with FOXM1 in breast cancer cells and they regulate ERα gene transcription [117]. There is a mutual regulatory mechanisms exist between FOXO3a and other FOX members. In glioblastoma brain tumor cells, SMAD3 is activated by transforming growth factor-β (TGF β) and that forms a complex with FOXO3a to induce the expression of growth inhibitory gene such as p21^Cip1, while FOXG1 binds to FOXO3a-SMAD3 complex and blocks p21^Cip1 expression [118]. In this context, the potential interaction between different FOX proteins make more complications in understanding the effects of FOX proteins on tumorigenesis. In other way, their interaction provide a point of integration for divergent signaling pathways that could be utilized for the effective therapy.

FOXO3a as biomarker and therapeutic target in cancer

Currently, due to the physiological and anatomical features of tumor, it is difficult to observe obvious early symptoms of patients, leading to a large number of patients diagnosed at an advanced stage. Therefore, valuable biomarkers for early diagnosis and prognosis of cancer are required in clinical practice. FOXO3a has recently emerged as a potential biomarker for the diagnosis, prognosis and treatment of multiple malignant tumors. For example, FOXO3a expression is identified as a cancer-initiating cells biomarker in Hodgkin’s lymphoma [119]. Many studies showed that FOXO3a expression acts as a prognostic biomarker in multiple cancers [94, 98, 120–127]. Interestingly, overexpression of FOXO3a is associated with poor prognosis in triple-negative breast cancer [120], hepatocellular carcinoma [121], glioblastoma [94] and gastric cancer [122] patients, whereas low expression of FOXO3a is associated with poor prognosis in glioma [126] and ovarian cancer [127] patients. The expression of phosphorylated FOXO3a is also identified as a prognostic biomarker in ovarian cancer [128] and acute myeloid leukemia [129]. The nuclear localization of FOXO3a is demonstrated as a prognostic biomarker in luminal-like breast cancer [130]. In addition, the subcellular localization of FOXO3a is identified as a biomarker for predicting response to the chemotherapy and radiotherapy in cervical carcinoma, breast cancer and esophageal cancer [131, 132]. Although the potential value of FOXO3a as a biomarker has been established in small-scale studies, it is difficult to validate it in large cohorts of patients with cancer. Therefore, further large-scale studies on patient populations are required to confirm the utility of FOXO3a as a biomarker in cancer.

FOXO3a has become a potential target of chemotherapeutic drugs due to its central role in in carcinogenesis. Many chemical and pharmacological agents targeting FOXO3a have been tested in clinical as well as experimental settings. FOXO3 is an indirect target of BMS-345541 (a highly selective IKK inhibitor) in T-cell acute lymphoblastic leukemia (T-ALL) in which the expression of p21^Cip1 is up-regulation by increased nuclear translocation of FOXO3a after treatment with BMS-345541. This process is independent of PKB and ERK 1/2 signaling, which indicates that the loss of FOXO3a tumor suppressor function could be mainly due to overactivation of IKK [133]. In BCR-ABL-positive chronic myeloid leukaemia cell lines, STI571 (also called imatinib or Glivec), an inhibitor of BCR-ABL oncoprotein, increases FOXO3a mediated apoptosis by triggering FOXO3a dependent cell cycle arrest and Bim expression [134]. Epigallocatechin-3-gallate (EGCG), the major constituent of green tea, can induce apoptosis by targeting FOXO3a in pancreatic carcinoma [135] and breast carcinoma cells [136]. FOXO3a is also an indirect target of many anticancer agents including paclitaxel [137], cisplatin [138], imatinib [139] and lidamycin [140] in breast cancer cells. All these compounds activate FOXO3a by decreasing PKB activity. However, Paclitaxel also enhances JNK activity, which targets both FOXO3a and 14–3-3 proteins. JNK regulates the activity or stability of FOXO3a by phosphorylation, and this phosphorylation event additionally reduces its interaction with 14–3-3 proteins, which results in the nuclear export of FOXO3a.

The PI3K-PKB pathway is a major downstream signaling pathway of epidermal growth factor receptor (EGFR), which is a crucial cell surface receptor involved in cancer cell proliferation. Thus, the inhibition of EGFR by chemotherapeutic drugs (trastuzumab, lapatinib, afatinib, cetuximab, gefitinib and neratinib) provide a novel and valuable therapeutic strategy for treating breast, colon, prostate, ovarian, lung and head and neck cancers [141, 142] by replenishing the activity of FOXO3a through inhibition of PI3K-PKB. BNIP3L is a pro-apoptotic gene, which is required for chemosensitization of cancer cells. This gene is one of the targets of FOXO3a. In breast cancer cell lines, the blockade of EGFR by antibodies or small-molecule inhibitors induces nuclear translocation of FOXO3a and promotes the expression of BNIP3L gene, which consequently results in apoptotic death of breast cancer cells [143]. Knockdown of FOXO3a also promotes the response to cetuximab treatment in colorectal cancer [144]. These findings indicate that FOXO3a could be a crucial target of small-molecule EGFR inhibitors, and its activity also increases chemosensitivity of cancer cells to agents such as lapatinib. In agreement with this, the activation of FOXO3a by other anticancer agents also sensitize cancer cells with resistance to apoptosis. For instance, FOXO3a transcriptional activity and its target gene Bim expression level is increased in Saos2 (a p53-null osteosarcoma cell line) upon ionizing radiation, which indicates that FOXO3a is a crucial effector of radiation-inducing apoptosis [100]. However, there is a drawback in therapeutically targeting FOXO3a for some type of cancers. IGFR1 and PI3KCA have been identified as target genes of FOXO3a in a colon carcinoma cell line [115], which indicates that FOXO3a may activate PI3K–PKB signaling pathway by multiple mechanisms and it could contribute to drug resistance in colon cancer. However, the majority of studies have revealed that the activation of FOXO3a is highly associated with apoptotic pathway in tumor cells.

FOXO3a activity is directly regulated by a large number of miRNAs. This indicates that the screening or synthesis of novel chemotherapeutic drugs targeting these miRNAs may also be a valuable strategy to treat cancer. Although valuable progress has been made in FOXO3a-based therapeutics for cancer, the most important challenges such as the detailed mechanism of FOXO3a in sensitivity and resistance of chemotherapeutic drugs remain to be solved before its translation in to clinic.

Conclusions

FOXO3a is a core regulator of multiple physiological and pathological processes by directly inducing or mediating the expression of genes associated with cell proliferation, growth and survival. The deregulation of FOXO3a signaling significantly contributes to the development and progression of many disorders, including cancer. There is a complicated cross-talk between FOXO3a and other key signaling pathways (such as p53 and ER) involved in carcinogenesis. Therefore, FOXO3a is a valuable therapeutic target for a wide range of cancers. The unique role of FOXO3a in the carcinogenesis is that certain tissues offers exciting possibility for cancer-tissue-specific therapeutic strategies. Current studies have shown that FOXO3a targeted chemotherapy has lower toxicity in normal tissues compared with tumor tissues. In chemotherapy-resistant breast cancer cell lines, FOXO3a activation is vital for sensitizing cells to chemotherapeutic agents. ERα is a critical regulator in breast cancer development and it is an efficient target for endocrine therapy [145]. The expression of ERα is considered as a marker for favorable prognosis and the level of functional ERα plays a key role in a successful endocrine treatment for breast cancer [146]. It is well documented that FOXO3a and FOXM1 regulate the expression of ERα [117]. Thus, FOXO3a could be a critical factor in determining the sensitivity and resistance of endocrine treatment. The PI3K-PKB signaling pathway is a relatively stable signaling pathway, which is not commonly mutated in cancers. Therefore, it is a promising strategy to identify novel inhibitors of FOXO3a for future anti-cancer drug design by targeting a downstream node of the PI3K-PKB pathway. As FOXO3a requires the recruitment of co-activators or suppressor for its activity or its inactivation, the therapeutic targeting of the coactivators or corepressors of FOXO3a could also be another way to manipulate FOXO3a functions in cancer cells. This strategy, along with therapeutic manipulation of PTM of FOXO3a would help to avoid the potential side effects in long term due to total inhibition of FOXO3a, which is required for normal cell functions. Given the fact that FOXO3a network is complex and considering its crosstalk with other transcription factors, the influence of FOXO3a in carcinogenesis need to be further investigated in order to develop an efficient FOXO3a based therapeutic strategies. The clinical applications of FOXO3a are potentially promising to limit the progression of human cancers in the future.

Abbreviations

3′ UTR

3′-untranslated region

AD

alzheimer’s Alzheimer’s disease

Aβ

AD amyloidAmyloid-β peptide

CARM1

coactivatorCoactivator-associated arginine methyltransferase 1

CBP

CREB-binding protein

CHOP

C/EBP homologous protein

DR

death Death receptor

EGCG

epigallocatechinEpigallocatechin-3-gallate

EGFR

epidermal Epidermal growth factor receptor

ERK

extracellular Extracellular signal-regulated kinase

ERα

estrogen Estrogen receptor α

FKH

forkhead Forkhead winged helix-turn-helix

FKHRL1

forehead Forehead in rhabdomyosarcoma-like 1

FLT3

fmsFms-like tyrosine kinase-3

FOX

forkhead Forkhead box

FOXO

forkhead Forkhead box class O

IBP

interferon Interferon regulatory factor-4 binding protein

IKKβ

IκB kinase isoform β

ITD

internal Internal tandem duplications

LANA2

latency Latency associated nuclear antigen 2

LBD

lewy Lewy body dementia

miRNA

microRNA

MST1

macrophage Macrophage stimulating 1

NES

nuclear Nuclear export sequence

NFκB

nuclear Nuclear factor κB

NLS

nuclear Nuclear localization sequence

NPM-ALK

nucleophosminNucleophosmin–anaplastic lymphoma; kinase

PD

pParkinson'’s disease

PI3K

phosphoinositolPhosphoinositol-3-kinase

PKB

protein Protein kinase B

POF

premature Premature ovarian failure

PTEN

phosphatase Phosphatase and tensin homologue deleted on chromosome 10

PTMs

postPost-translational modifications

SGK

serumSerum-and glucocorticoid-inducible kinases

TAD

transactivation Transactivation domain

T-ALL

t-cell acute lymphoblastic leukemia

TGF β

transforming Transforming growth factor-β

Authors’ contributions

WD, WW, XDH, WPY and YFW collected the related paper. YL and XA drafted and wrote the manuscript. MP revised the manuscript. JXW and PFL participated in the design of the review and helped to draft and revise the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

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